Analytical Chemistry · 2017 · 119 citations · 27 references
EngineeringBiomedical EngineeringBiotechnologyBiophysical ChemistryBiosensorsNanobiotechnologyDna BiosensorsDna NanotechnologyMolecular SensorsNanosensorsNucleic Acid BiosensorsSignal Amplification StrategiesBiosensor DevelopmentCatalytic Hairpin AssemblyCatalyzed Hairpin AssemblyDna SensorsHydroxyl Radical ChemistryMucin GlycoproteinsProbe DetectionUltrasensitive Detection
Herein, we fabricated a novel electrochemiluminescence (ECL) biosensor for ultrasensitive detection of mucin 1 (MUC1) based on a three-dimensional (3-D) DNA nanomachine signal probe powered by protein-aptamer binding complex. The assembly of 3-D DNA nanomachine signal probe achieved the cyclic reuse of target protein based on the protein-aptamer binding complex induced catalyzed hairpin assembly (CHA), which overcame the shortcoming of protein conversion with enzyme cleavage or polymerization in the traditional examination of protein. In addition, CoFe 2 O 4, a mimic peroxidase, was used as the nanocarrier of the 3-D DNA nanomachine signal probe to catalyze the decomposition of coreactant H 2 O 2 to generate numerous reactive hydroxyl radical OH • as the efficient accelerator of N -(aminobutyl)- N -(ethylisoluminol) (ABEI) ECL reaction to amplify the luminescence signal. Simultaneously, the assembly of 3-D DNA nanomachine signal probe was executed in solution, which led to abundant luminophore ABEI be immobilized around the CoFe 2 O 4 surface with amplified ECL signal output since the CHA reaction was occurred unencumberedly in all directions under homogeneous environment. The prepared ECL biosensor showed a favorable linear response for MUC1 detection with a relatively low detection limit of 0.62 fg mL –1 . With excellent sensitivity, the strategy may provide an efficient method for clinical application, especially in trace protein determination.
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